1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride

Base Information

Chemical Name:1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride
CAS No.:114185-22-7
Molecular Formula:C₂₆H₃₀N₂O₅*2ClH
Molecular Weight:523.456
Hs Code.:

Synonyms:1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride

Suppliers and Price of 1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride

There total 2 articles about 1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 82.4%

: 114185-29-4
1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-bis(benzyloxy)-1,2,3,4-tetrahydroisoquinoline

: 114185-22-7
1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride

Guidance literature:: With hydrogenchloride; In methanol; for 3.5h;
DOI:10.1021/jm00403a006

Reference yield:

: 114197-87-4
1-(3,4,5-trimethoxybenzyl)-2-(4-nitrobenzyl)-6,7-bis(benzyloxy)-1,2,3,4-tetrahydroisoquinoline oxalate

: 114185-22-7
1-(3,4,5-trimethoxybenzyl)-2-(4-aminobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: stannous chloride, conc. HCl / ethanol / 0.75 h / Heating

2: 82.4 percent / conc. HCl / methanol / 3.5 h

With hydrogenchloride; tin(ll) chloride; In methanol; ethanol;
DOI:10.1021/jm00403a006